| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.211673250G>A | CA16602254 | ERBB4 | c.1630C>T (p.Arg544Trp) c.1552C>T (p.Arg518Trp) c.1629C>T c.1453C>T (p.Arg485Trp) n.1682C>T c.1708C>T (p.Arg570Trp) c.1009C>T (p.Arg337Trp) | ClinVar dbSNP gnomAD v4 COSMIC |
| 2 | g.211673250G= | CA1325600470 | ERBB4 | c.1630C= (p.Arg544=) c.1552C= (p.Arg518=) c.1629C= c.1453C= (p.Arg485=) n.1682C= c.1708C= (p.Arg570=) c.1009C= (p.Arg337=) | dbSNP |